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Sedation practices in adult patients with severe ARDS on extracorporeal respiratory support using VV ECMO - An international survey. VV ECMO体外呼吸支持下严重急性呼吸窘迫综合征(ARDS)成年患者镇静治疗的国际调查
IF 1.1 4区 医学 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-14 DOI: 10.1177/02676591251415338
Christopher Noel, Adam Green, Abhimanyu Chandel, Joseph Delio, Nitin Puri, Chase Donaldson, Craig Rackley, Steven A Conrad, Peter Rycus, Joseph E Tonna, Akram Zaaqoq, Justyna Swol, Christopher King

IntroductionOptimal sedation strategies for patients with respiratory failure requiring venovenous extracorporeal membrane oxygenation (VV ECMO) are not well defined.MethodsPhysicians caring for patients on ECMO in an intensive care unit were invited to complete an international survey about sedation and analgesia practices for adult patients undergoing VV ECMO for severe Acute Respiratory Distress Syndrome (ARDS).ResultsThe survey was completed by 234 physicians, most commonly identifying as critical care (29.9%) and practicing in North America (38.9%). The Richmond Agitation Sedation Scale (88.5%) and Clinical Pain Observation Tool (40.2%) were commonly used for monitoring. Agents of choice were propofol (73.9% prior to ECMO and 56% within 48 h after initiation) and fentanyl (57.3% and 40.2%), with increasing preference for dexmedetomidine after ECMO initiation (14.5% prior to and 25.6% after initiation). Routine neuromuscular blockade use beyond 48 h after cannulation was rare (1.3%). Common strategies to reduce sedatives included sweep gas titration (74.4%) and minimizing nocturnal interventions (63.7%). Most respondents believe antipsychotics also work to this effect (57.3%).ConclusionsSedation strategies for adult ARDS patients receiving VV ECMO seem to be influenced by time from cannulation and patient factors. Future research should focus on identifying optimal sedation strategies and developing a consensus for best practice.

需要静脉-静脉体外膜氧合(VV ECMO)的呼吸衰竭患者的最佳镇静策略尚未明确。方法邀请重症监护病房(icu) ECMO患者的护理医师完成一项关于VV ECMO治疗严重急性呼吸窘迫综合征(ARDS)成人患者镇静镇痛做法的国际调查。结果该调查由234名医生完成,最常见的是重症监护(29.9%)和北美执业(38.9%)。常用的监测方法为Richmond躁动镇静量表(88.5%)和临床疼痛观察工具(40.2%)。选择的药物是异丙酚(ECMO前73.9%,开始后48 h内56%)和芬太尼(57.3%,40.2%),ECMO开始后右美托咪定的偏好增加(开始前14.5%,开始后25.6%)。插管后超过48小时常规使用神经肌肉阻断剂的情况很少见(1.3%)。减少镇静剂的常用策略包括扫气滴定(74.4%)和尽量减少夜间干预(63.7%)。大多数受访者认为抗精神病药物也有这种效果(57.3%)。结论VV ECMO对成年ARDS患者的镇静策略可能受插管时间和患者因素的影响。未来的研究应侧重于确定最佳镇静策略,并就最佳实践达成共识。
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引用次数: 0
Investigating cannula tip angles in pulmonary artery ECMO: A computational study on the potential benefits of angulation for oxygen delivery. 肺动脉ECMO中导管尖端角度的研究:角度对氧气输送的潜在益处的计算研究。
IF 1.1 4区 医学 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-13 DOI: 10.1177/02676591251407293
Eiman Shah, Jan Spillner, Johannes Greven, Annika Schmitz, Andreas Horbach, Yvan Fournier, Mehdi Behbahani

IntroductionPulmonary artery (PA) cannulation is emerging as a method for concurrent cardiac and respiratory failure, but limited data exists on how cannula positioning, particularly cannula tip angle, affects perfusion symmetry. Due to varying pulmonary bifurcation geometry between patients, ensuring even distribution of oxygen-saturated blood becomes critical. This computational fluid dynamics (CFD) study investigated the effects of cannula positioning and angles on oxygen delivery within the PA using 6 different configurations.MethodAn idealized PA geometry based on a CT scan was constructed including the 6 different cannula configurations: two straight (short and long) and four angled (5° and 10° toward either pulmonary branch). Simulations assumed laminar, steady-state flow at 6 L/min total (50% ECMO contribution). Oxygen transport was modeled as a passive scalar with 75% saturation from the heart and 100% from the cannula. Perfusion symmetry was quantified using the absolute difference in mean oxygen saturation (ΔSaO2) and partial pressure (ΔpO2) between the right (RPA) and left pulmonary arteries (LPA).ResultsCannula positioning and angulation influences oxygen distribution within the PA. Straight-tipped cannulas favored LPA-sided flow due to the natural geometry of the pulmonary artery (ΔSaO2 = 12.9-15.1%). A 5° RPA directed angulation achieved the most symmetric distribution (ΔSaO2 = 9.2%, ΔpO2 = 14.2 mmHg), whereas greater or opposite angulations increased flow asymmetry.ConclusionMinor cannula tip angulation, specifically 5° deflection towards the RPA, enhances bilateral PA oxygenation without increasing ECMO flow, providing a simple yet effective strategy for optimizing pulmonary ECMO perfusion.

肺动脉插管(PA)正在成为治疗并发心力衰竭和呼吸衰竭的一种方法,但关于插管位置,特别是导管尖端角度如何影响灌注对称性的数据有限。由于患者之间肺分叉的几何形状不同,确保饱和氧血的均匀分布变得至关重要。计算流体动力学(CFD)研究了6种不同配置的导管位置和角度对PA内氧气输送的影响。方法基于CT扫描构建理想的肺动脉几何形状,包括6种不同的插管配置:2种直(短和长)和4种角度(向肺分支5°和10°)。模拟假设层流,稳态流量为6l /min (ECMO贡献的50%)。氧运输建模为被动标量,其中75%的饱和度来自心脏,100%来自插管。通过右肺动脉(RPA)和左肺动脉(LPA)的平均氧饱和度(ΔSaO2)和分压(ΔpO2)的绝对差值来量化灌注对称性。结果扫描仪的位置和角度影响动脉血氧分布。由于肺动脉的自然几何形状,直端插管有利于lpa侧的血流(ΔSaO2 = 12.9-15.1%)。5°RPA定向成角实现了最对称的分布(ΔSaO2 = 9.2%, ΔpO2 = 14.2 mmHg),而更大的或相反的成角会增加流动的不对称性。结论微小的导管尖端成角,特别是向RPA偏转5°,可在不增加ECMO流量的情况下增强双侧PA氧合,为优化肺ECMO灌注提供了一种简单而有效的策略。
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引用次数: 0
Correlation of anticoagulation assays with bleeding during extracorporeal membrane oxygenation at a tertiary pediatric hospital. 一家三级儿科医院体外膜氧合期间抗凝试验与出血的相关性
IF 1.1 4区 医学 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-13 DOI: 10.1177/02676591261417542
Mohammed Salameh, Jazmin Delgado, Ryan Killebrew, Cody Henderson, Elumalai Appachi

IntroductionDue to anticoagulation during Extracorporeal Membrane Oxygenation (ECMO), patients face a higher risk of bleeding. This study aimed to assess the correlation between anticoagulation assays and hemorrhage in ECMO patients.MethodsWe reviewed records from patients in our critical care units, comparing anticoagulation parameters with clinical outcomes. Statistical analyses included the Wilcoxon rank sum test for continuous variables and chi-square or Fisher's exact tests for categorical variables. We used Kaplan-Meier curves to depict hemorrhage incidence and logistic regression to identify factors associated with bleeding and mortality. Linear regression assessed coagulation factors linked to length of stay (LOS).ResultsOf 76 patients, 32 (42.1%) experienced hemorrhage; 15 (46.9%) of these survived. Survivors had a higher proportion without bleeding (68.2%). Hemorrhage patients had more circuit changes (18.8% vs 2.3%, p = .01). The 10-, 20-, and 30-days cumulative hemorrhage incidences were 36.9%, 58.8%, and 72.5%, respectively. Multivariable analysis suggested that bleeding patients had a higher aPTT prior to the bleeding event compared with the median aPTT in non-bleeding patients (p = 0.04), and ACT and PT levels showed a trend towards a significant association (p = 0.06). Longer ECMO runs and circuit changes increased hemorrhage risk (OR = 1.004 and OR = 12.85, respectively).ConclusionOur study found that higher aPTT and longer ECMO duration are independent hemorrhage risk factors, underscoring the need for timely ECMO decannulation.

由于体外膜氧合(ECMO)期间的抗凝,患者面临更高的出血风险。本研究旨在评估ECMO患者抗凝试验与出血的相关性。方法回顾重症监护病房患者的记录,比较抗凝参数与临床结果。统计分析包括对连续变量的Wilcoxon秩和检验和对分类变量的卡方检验或Fisher精确检验。我们使用Kaplan-Meier曲线来描述出血发生率,并使用逻辑回归来确定与出血和死亡率相关的因素。线性回归评估与住院时间(LOS)相关的凝血因子。结果76例患者中,32例(42.1%)出现出血;15例(46.9%)存活。幸存者中无出血的比例较高(68.2%)。出血患者有更多的电路改变(18.8% vs 2.3%, p = 0.01)。10天、20天和30天的累计出血发生率分别为36.9%、58.8%和72.5%。多变量分析显示,出血患者出血前aPTT高于非出血患者的中位aPTT (p = 0.04), ACT和PT水平呈显著相关趋势(p = 0.06)。较长的ECMO运行和回路改变增加出血风险(OR分别为1.004和12.85)。结论aPTT升高和ECMO持续时间延长是独立的出血危险因素,需要及时进行ECMO脱管。
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引用次数: 0
Securing data management systems in perfusion: A narrative review on cybersecurity and clinical risk. 灌注保护数据管理系统:网络安全和临床风险的叙述性回顾。
IF 1.1 4区 医学 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-12 DOI: 10.1177/02676591261417526
Youssef El Dsouki, Ignazio Condello, Calogero Iacona, Samir El Daccache, Roberto Lorusso

BackgroundThe increasing digitization of perfusion practice has led to the integration of advanced data management systems (DMS) that record and analyze intraoperative variables in real time. While these systems improve accuracy, traceability, and clinical decision-making, they also expose perfusion workflows to significant cybersecurity risks. Given that perfusion data directly reflect artificial circulation, any loss of integrity or service can have immediate clinical consequences.Materials and MethodsA comprehensive narrative review was conducted to synthesize current knowledge on cybersecurity in perfusion informatics and performance. The research strategy combined systematic database searches (PubMed, Scopus, IEEE Xplore, and Web of Science) with targeted grey literature review (regulatory frameworks and institutional reports). Inclusion criteria focused on articles published between 2010 and 2024 addressing healthcare cybersecurity, perfusion informatics, and medical device security. Studies were analyzed qualitatively to identify recurring themes, technological approaches, and governance models. Reference cross-checking ensured comprehensive coverage, and terminology was standardized according to ISO/IEC 27001 principles. The review followed an integrative, non-meta-analytic design, emphasizing conceptual synthesis rather than statistical aggregation.ResultsThirty-three primary and secondary sources were identified. The literature reveals a consistent pattern of vulnerabilities across clinical DMS, with perfusion systems being particularly exposed to ransomware, data tampering, and service interruption. The review highlights the centrality of the Confidentiality-Integrity-Assurance of Service triad as a guiding model. Key strategies identified include encryption and role-based access control, blockchain audit trails, federated learning, and post-quantum cryptography. However, empirical studies focusing specifically on perfusion remain scarce, underscoring a major research gap.ConclusionsCybersecurity in perfusion informatics must evolve from a technical adjunct to a clinical mandate. Integrating security frameworks into perfusion workflows supported by legal compliance (HIPAA, GDPR, ISO 27001) and ethical governance is essential to preserve patient safety. Future research should prioritize multicenter simulations, resilience testing, and cross-disciplinary training to ensure the continuity, integrity, and trustworthiness of digital perfusion systems.

灌注实践的日益数字化导致了先进的数据管理系统(DMS)的集成,可以实时记录和分析术中变量。虽然这些系统提高了准确性、可追溯性和临床决策,但它们也使灌注工作流程面临重大的网络安全风险。鉴于灌注数据直接反映人工循环,任何完整性或服务的损失都可能导致直接的临床后果。材料与方法对灌注信息学和性能方面的网络安全知识进行了全面的综述。研究策略结合了系统的数据库搜索(PubMed, Scopus, IEEE Xplore和Web of Science)和有针对性的灰色文献综述(监管框架和机构报告)。纳入标准侧重于2010年至2024年间发表的关于医疗保健网络安全、灌注信息学和医疗设备安全的文章。对研究进行定性分析,以确定反复出现的主题、技术方法和治理模型。参考交叉检查确保全面覆盖,术语根据ISO/IEC 27001原则标准化。本综述采用综合、非元分析设计,强调概念综合而非统计汇总。结果共鉴定了33个一级和二级来源。文献揭示了临床DMS中一致的漏洞模式,灌注系统特别容易受到勒索软件、数据篡改和服务中断的影响。该审查强调了作为指导模式的保密性-完整性-服务保证三位一体的中心地位。确定的关键策略包括加密和基于角色的访问控制、区块链审计跟踪、联邦学习和后量子加密。然而,专门针对灌注的实证研究仍然很少,这凸显了一个重大的研究空白。结论灌注信息学中的网络安全必须从技术辅助发展到临床任务。在法律合规(HIPAA、GDPR、ISO 27001)和道德治理的支持下,将安全框架集成到灌注工作流程中,对于保护患者安全至关重要。未来的研究应优先考虑多中心模拟、弹性测试和跨学科培训,以确保数字灌注系统的连续性、完整性和可靠性。
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引用次数: 0
Prediction of primary graft dysfunction and survival in heart transplantation using normothermic ex-vivo perfusion of the donor heart. 利用供体心脏常温离体灌注预测心脏移植的原发性移植物功能障碍和存活。
IF 1.1 4区 医学 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-09 DOI: 10.1177/02676591251413738
Julius Borger, Marion Bäuerlein, Michael Berchtold-Herz, Matthias Eschenhagen, Thilo Fleck, Gerd Haimerl, Christoph Benk, Friedhelm Beyersdorf, Martin Czerny, Sven Maier, David Schibilsky

IntroductionEx vivo perfusion (EVP) in heart transplantation (HTX) enables transportation of explanted organs over longer distances as well as monitoring of cardiac metabolism under unloaded coronary perfusion, thereby expanding the possible pool of suitable donors for HTX. We aimed at identifying possibly modifiable risk factors predicting impaired outcome after HTX through analysis of perfusion parameters, donor and recipient characteristics.MethodsWe included 64 patients after HTX using EVP (TransMedics Organ Care System) between February 2010 and October 2022 in this retrospective, single-center analysis. Blood gas analyses were taken during EVP in a standardized manner.ResultsHTX recipients were 44.8 ± 16.2 years old, six patients being younger than 18 years at the time of transplantation. High urgency listing status was present in 79.7%, and 67.2% had previous cardiac surgery. Lower base excess during EVP predicted severe primary graft dysfunction (PGD) (-5.55 ± 1.95 vs -3.94 ± 2.38 mmol/L, p = 0.043). With every additional minute of warm ischemia, the risk of PGD was 3.7% higher (OR 1.037, 95% CI [1.004; 1.072], p = 0.028). Low donor serum potassium (3.4 ± 0.76 mmol/L vs 4.2 ± 0.60, p = 0.008), high glucose after EVP priming (207.63 ± 99.05 mg/dL vs 146.45 ± 51.99, p = 0.045), and resuscitation of the donor (55.6% vs 18.2%, p = 0.027) were associated with impaired survival after HTX.ConclusionsEVP provides a unique method to assess graft function during the retrieval of hearts for cardiac transplantation. Low base excess, priming glucose, warm ischemia and donor hypokalaemia influence the frequency of adverse outcomes after HTX. Future studies may address possible strategies to safely modify these risk factors.

心脏移植(HTX)中的体外灌注(EVP)可以使移植器官在更远的距离上运输,并在无负荷冠状动脉灌注下监测心脏代谢,从而扩大了HTX合适供体的可能来源。我们旨在通过分析灌注参数、供体和受体特征,确定预测HTX后预后受损的可能可改变的危险因素。方法在2010年2月至2022年10月期间,我们纳入64例使用TransMedics器官护理系统(EVP)接受HTX治疗的患者,进行回顾性单中心分析。在EVP过程中以标准化的方式进行血气分析。结果shtx受者年龄为44.8±16.2岁,6例患者移植时年龄小于18岁。79.7%的患者处于高度紧急状态,67.2%的患者既往有心脏手术史。EVP期间较低的碱过量预测严重的原发性移植物功能障碍(PGD)(-5.55±1.95 vs -3.94±2.38 mmol/L, p = 0.043)。每增加1分钟的热缺血,PGD的风险增加3.7% (OR 1.037, 95% CI [1.004; 1.072], p = 0.028)。低供体血钾(3.4±0.76 mmol/L vs 4.2±0.60,p = 0.008)、EVP启动后高葡萄糖(207.63±99.05 mg/dL vs 146.45±51.99,p = 0.045)和供体复苏(55.6% vs 18.2%, p = 0.027)与HTX术后生存受损相关。结论sevp为心脏移植取心过程中评估移植物功能提供了一种独特的方法。低碱过量、启动葡萄糖、热缺血和供体低钾血症影响HTX后不良结局的发生频率。未来的研究可能会解决可能的策略,以安全地改变这些危险因素。
{"title":"Prediction of primary graft dysfunction and survival in heart transplantation using normothermic ex-vivo perfusion of the donor heart.","authors":"Julius Borger, Marion Bäuerlein, Michael Berchtold-Herz, Matthias Eschenhagen, Thilo Fleck, Gerd Haimerl, Christoph Benk, Friedhelm Beyersdorf, Martin Czerny, Sven Maier, David Schibilsky","doi":"10.1177/02676591251413738","DOIUrl":"https://doi.org/10.1177/02676591251413738","url":null,"abstract":"<p><p>IntroductionEx vivo perfusion (EVP) in heart transplantation (HTX) enables transportation of explanted organs over longer distances as well as monitoring of cardiac metabolism under unloaded coronary perfusion, thereby expanding the possible pool of suitable donors for HTX. We aimed at identifying possibly modifiable risk factors predicting impaired outcome after HTX through analysis of perfusion parameters, donor and recipient characteristics.MethodsWe included 64 patients after HTX using EVP (TransMedics Organ Care System) between February 2010 and October 2022 in this retrospective, single-center analysis. Blood gas analyses were taken during EVP in a standardized manner.ResultsHTX recipients were 44.8 ± 16.2 years old, six patients being younger than 18 years at the time of transplantation. High urgency listing status was present in 79.7%, and 67.2% had previous cardiac surgery. Lower base excess during EVP predicted severe primary graft dysfunction (PGD) (-5.55 ± 1.95 vs -3.94 ± 2.38 mmol/L, <i>p</i> = 0.043). With every additional minute of warm ischemia, the risk of PGD was 3.7% higher (OR 1.037, 95% CI [1.004; 1.072], <i>p</i> = 0.028). Low donor serum potassium (3.4 ± 0.76 mmol/L vs 4.2 ± 0.60, <i>p</i> = 0.008), high glucose after EVP priming (207.63 ± 99.05 mg/dL vs 146.45 ± 51.99, <i>p</i> = 0.045), and resuscitation of the donor (55.6% vs 18.2%, <i>p</i> = 0.027) were associated with impaired survival after HTX.ConclusionsEVP provides a unique method to assess graft function during the retrieval of hearts for cardiac transplantation. Low base excess, priming glucose, warm ischemia and donor hypokalaemia influence the frequency of adverse outcomes after HTX. Future studies may address possible strategies to safely modify these risk factors.</p>","PeriodicalId":49707,"journal":{"name":"Perfusion-Uk","volume":" ","pages":"2676591251413738"},"PeriodicalIF":1.1,"publicationDate":"2026-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145946705","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Hyperthermic Extracorporeal Applied Tumor Therapy (HEATT®) in hospice- eligible cancer patients. 热体外应用肿瘤治疗(HEATT®)在符合临终关怀的癌症患者中的应用。
IF 1.1 4区 医学 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-08 DOI: 10.1177/02676591251413475
Joseph B Zwischenberger, Peyton Mashni, Robert Fischer, Joanne Essa, Sarah Hatchett, Jan Winetz, Roger Vertrees

BackgroundTwo previous clinical studies indicated veno-venous perfusion-induced systemic hyperthermia (VV-PISH), producing elevated temperatures of 42°C, induces cell death, apoptosis, or senescence of responsive cancers. The VV-PISH circuit has been refined and rebranded as Hyperthermic Extracorporeal Applied Tumor Treatment (HEATT®).MethodsThe local IRB approved this retrospective chart review. All devices are FDA-approved. The referring physician judged each patient to be hospice-eligible with a median predicted survival of 3 months and maximum predicted survival of 6 months. We evaluated HEATT® in hospice-eligible patients (n = 13) with unresponsive, advanced cancer, conducted at a single site, with a select, consistent team of healthcare providers (critical care, anesthesia, perfusionist, interventional radiologist, HEATT® consultant). HEATT® treatment (42°C for 120 min) was delivered once between June 2021 and April 2022. The referring physician followed patients until documented death. HEATT circuit and criteria were refined to maximize safety.ResultsIn a retrospective chart review of the 13 consecutive patients, 8/13 patients exceeded expected median survival, 6/13 exceeded the 6-months predicted end-of-life, and 5/13 exceeded 12 months. Lessons learned allowed the refinement of inclusion/exclusion criteria of Karnofsky >70, ability to ambulate, and age <80. Likewise, refining the circuitry led to improved standardization of the HEATT® perfusion technique and management.ConclusionsThis consecutive series of 13 hospice-eligible patients demonstrated the refinement of HEATT®, focusing on perfusion technique and selection criteria. In this small series of physician-referred hospice-eligible patients unresponsive to conventional therapy or other integrative oncology treatments, HEATT® demonstrated safety with an increase in the length of survival over median expected in eight of 13 patients, with five of 13 patients living 12 to 18 months, 2-3 times longer than the referring physician expected. These refinements are essential to enable prospective randomized trials of like-patient populations to generate evidence-based medical recommendations.

先前的两项临床研究表明,静脉-静脉灌注诱导的全身热疗(VV-PISH),产生42°C的升高温度,诱导细胞死亡、凋亡或应答性癌症衰老。VV-PISH电路已被改进并重新命名为高温体外应用肿瘤治疗(HEATT®)。方法本回顾性病历经当地IRB批准。所有设备都是fda批准的。转诊医师以中位预估生存期为3个月,最大预估生存期为6个月来判断每位病人是否符合安宁疗护条件。我们对符合临终关怀条件的无反应晚期癌症患者(n = 13)进行了HEATT®评估,在单一地点进行,由精选的、一致的医疗保健提供者团队(重症监护、麻醉、灌注师、介入放射科医生、HEATT®顾问)组成。HEATT®处理(42°C 120分钟)在2021年6月至2022年4月期间交付一次。转诊医生对患者进行随访,直到有死亡记录。HEATT电路和标准经过改进,以最大限度地提高安全性。结果对连续13例患者进行回顾性图表回顾,8/13例患者超过预期中位生存期,6/13例超过6个月预测终期,5/13例超过12个月。吸取的经验教训允许细化Karnofsky bbb70的纳入/排除标准,行走能力和age®灌注技术和管理。结论连续13例符合临终关怀条件的患者展示了HEATT®的改进,重点是灌注技术和选择标准。在这个小范围的医生推荐的符合临终关怀条件的患者中,对传统治疗或其他综合肿瘤治疗无反应,13名患者中有8名患者的生存期超过预期中值,13名患者中有5名患者的生存期为12至18个月,比转诊医生预期的时间长2-3倍。这些改进对于使对类似患者群体的前瞻性随机试验产生循证医学建议至关重要。
{"title":"Hyperthermic Extracorporeal Applied Tumor Therapy (HEATT<sup>®</sup>) in hospice- eligible cancer patients.","authors":"Joseph B Zwischenberger, Peyton Mashni, Robert Fischer, Joanne Essa, Sarah Hatchett, Jan Winetz, Roger Vertrees","doi":"10.1177/02676591251413475","DOIUrl":"https://doi.org/10.1177/02676591251413475","url":null,"abstract":"<p><p>BackgroundTwo previous clinical studies indicated veno-venous perfusion-induced systemic hyperthermia (VV-PISH), producing elevated temperatures of 42°C, induces cell death, apoptosis, or senescence of responsive cancers. The VV-PISH circuit has been refined and rebranded as Hyperthermic Extracorporeal Applied Tumor Treatment (HEATT<sup>®</sup>).MethodsThe local IRB approved this retrospective chart review. All devices are FDA-approved. The referring physician judged each patient to be hospice-eligible with a median predicted survival of 3 months and maximum predicted survival of 6 months. We evaluated HEATT<sup>®</sup> in hospice-eligible patients (<i>n</i> = 13) with unresponsive, advanced cancer, conducted at a single site, with a select, consistent team of healthcare providers (critical care, anesthesia, perfusionist, interventional radiologist, HEATT<sup>®</sup> consultant). HEATT<sup>®</sup> treatment (42°C for 120 min) was delivered once between June 2021 and April 2022. The referring physician followed patients until documented death. HEATT circuit and criteria were refined to maximize safety.ResultsIn a retrospective chart review of the 13 consecutive patients, 8/13 patients exceeded expected median survival, 6/13 exceeded the 6-months predicted end-of-life, and 5/13 exceeded 12 months. Lessons learned allowed the refinement of inclusion/exclusion criteria of Karnofsky >70, ability to ambulate, and age <80. Likewise, refining the circuitry led to improved standardization of the HEATT<sup>®</sup> perfusion technique and management.ConclusionsThis consecutive series of 13 hospice-eligible patients demonstrated the refinement of HEATT<sup>®</sup>, focusing on perfusion technique and selection criteria. In this small series of physician-referred hospice-eligible patients unresponsive to conventional therapy or other integrative oncology treatments, HEATT<sup>®</sup> demonstrated safety with an increase in the length of survival over median expected in eight of 13 patients, with five of 13 patients living 12 to 18 months, 2-3 times longer than the referring physician expected. These refinements are essential to enable prospective randomized trials of like-patient populations to generate evidence-based medical recommendations.</p>","PeriodicalId":49707,"journal":{"name":"Perfusion-Uk","volume":" ","pages":"2676591251413475"},"PeriodicalIF":1.1,"publicationDate":"2026-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145935923","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Continuous or intermittant retrograde cardioplegia during coronary bypass: A propensity score adjusted comparison. 冠状动脉搭桥期间持续或间歇逆行性心脏骤停:倾向评分调整后的比较。
IF 1.1 4区 医学 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-08 DOI: 10.1177/02676591261416083
Kemal Uzun, Muhammet Onur Hanedan, Hakan Kara, Selma Fiş Topaloğlu

IntroductionContinuous retrograde cardioplegia worsens surgeon's vision while performing distal anastomosis in coronary artery bypass grafting operations. We investigated whether intermittent retrograde cardioplegia, which provides a bloodless surgical field by interrupting cardioplegia flow during distal anastomosis, poses a disadvantage in terms of myocardial protection.MethodsThis retrospective study was conducted in two different heart centres between January 2013 and July 2023. A total of 234 patients who underwent ≥2 target vessel revascularization under cardiopulmonary bypass were examined. Isothermic, potassium-enriched blood cardioplegia was used and induction was performed antegrade in all patients. In addition to antegrade, we routinely gave retrograde cardioplegia. Retrograde cardioplegia was applied continuously with the force of gravity in the continuous group (n = 167), and intermittently with pressure in the intermittent group (n = 167).ResultsThe volume of cardioplegia solution administered was significantly higher in the intermittent group compared to the continuous group (4070 ± 760 mL vs 3190 ± 575 mL; p = 0.001). However, no significant differences were observed between the groups regarding postoperative clinical outcomes or early mortality rates.ConclusionsIntermittent retrograde cardioplegia offers superior operative conditions by ensuring a bloodless surgical field and improved procedural comfort, while maintaining equivalent efficacy in myocardial protection compared with the continuous method.

在冠状动脉搭桥术中,持续逆行心脏截瘫使外科医生在远端吻合时视力下降。我们研究了间歇性逆行心脏骤停是否会在心肌保护方面造成不利影响,因为它在远端吻合过程中通过中断心脏骤停血流提供了无血的手术野。方法回顾性研究于2013年1月至2023年7月在两个不同的心脏中心进行。共有234例患者在体外循环下接受了≥2次靶血管重建术。采用等温富钾血停搏,所有患者行顺行诱导。除了顺行性外,我们还常规给予逆行性心脏骤停。逆行心脏骤停连续组(n = 167)连续施加重力,间歇组(n = 167)间歇施加压力。结果间歇组给药的停搏液量明显高于连续组(4070±760 mL vs 3190±575 mL; p = 0.001)。然而,在术后临床结果或早期死亡率方面,两组间没有观察到显著差异。结论间歇逆行心脏截瘫术具有良好的手术条件,保证了手术视野无血,提高了手术舒适性,同时保持了与连续方法相当的心肌保护效果。
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引用次数: 0
Nitric oxide delivery into the sweep flow of ECMO systems: Technical challenges and solutions. ECMO系统扫流中一氧化氮的输送:技术挑战和解决方案。
IF 1.1 4区 医学 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-06 DOI: 10.1177/02676591251408659
Adrian C Mattke, Kerry Johnson, Giles J Peek, Prem Venugopal, Steve Horton

Sweep gas nitric oxide (sNO) is emerging as an adjunctive therapy, which may have positive impacts on thrombosis and inflammation during ECMO treatment. sNO is administered to the gas phase of the ECMO oxygenator with the aim of reducing contact activation of blood when flowing through and over artificial surfaces. NO delivery devices have gas flow requirements that are above the sweep gases requirements of smaller patients supported on ECMO. To facilitate sNO delivery in patients requiring a sweep flow rate below the required bias flow rate of NO delivery devices, varying sNO delivery setups have been described. Here, we describe three systems for safe and reliable sNO delivery.

扫描气体一氧化氮(sNO)正在成为一种辅助治疗,可能对ECMO治疗期间的血栓形成和炎症产生积极影响。sNO被施用于ECMO氧合器的气相,目的是减少血液流过人工表面时的接触活化。NO输送装置的气体流量要求高于ECMO支持的较小患者的扫描气体要求。为了促进sNO在需要低于NO输送装置所需的偏置流量的扫描流速的患者中的输送,已经描述了不同的sNO输送设置。在这里,我们描述了三种安全可靠的sNO输送系统。
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引用次数: 0
Perfusionist's role in long-term ventricular assist device. 灌注师在长期心室辅助装置中的作用。
IF 1.1 4区 医学 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-05 DOI: 10.1177/02676591251415511
Yolly Gigliola Perea Bautista, Yadira Estrada García, Dafna García Gómez, Edgar Fabián Manrique-Hernández, Maricel Licht-Ardila, Alejandra Mendoza-Monsalve, Alexandra Hurtado-Ortiz, Gustavo Prieto, Leonardo Salazar

IntroductionVentricular assist devices (VADs) have emerged as essential tools for stage D heart failure, improving survival and quality of life by serving as a bridge to transplant, destination therapy, or bridge to decision. The successful implantation and management of VADs requires a multidisciplinary team, in which perfusionists have a critical role in ensuring proper oxygen delivery, hemodynamic support, and the smooth transition from extracorporeal support to the implanted device. The objective was to describe the institutional perfusion protocol for LVAD implantation and to characterize intraoperative perfusion parameters at a Latin American referral center.MethodsA retrospective observational cohort study was conducted including all patients who underwent LVAD implantation at a referral center in northeastern Colombia. Statistical analysis involved the use of descriptive statistics.ResultsA total of 33 patients underwent LVAD implantation, with a median age of 54 years and 51.52% of male. Ischemic cardiomyopathy was the leading etiology (27.27%). The median cardiopulmonary bypass (CPB) time was 153 min (IQR: 128-181). During cardiopulmonary bypass the median lactate levels were 1.8 mmol/L (IQR: 1.5-2.2), and the cardiac index ranged from a minimum CI of 2.3 to a maximum CI of 2.6 L/min/m2.ConclusionsThis study highlights the vital role of cardiopulmonary perfusion in the successful implantation of long-term LVADs in advanced heart failure patients. Optimal intraoperative management, including controlled temperature, low lactate levels, and optimal cardiac index, emphasizes the need for standardized strategies and the expertise of perfusionists.

心室辅助装置(vad)已成为D期心力衰竭的重要工具,通过作为移植、终点治疗或决策的桥梁,提高生存率和生活质量。VADs的成功植入和管理需要一个多学科的团队,其中灌注师在确保适当的氧气输送,血流动力学支持以及从体外支持到植入装置的顺利过渡方面发挥着关键作用。目的是描述LVAD植入的机构灌注方案,并描述拉丁美洲转诊中心术中灌注参数的特征。方法回顾性观察队列研究,纳入哥伦比亚东北部某转诊中心接受LVAD植入的所有患者。统计分析包括使用描述性统计。结果33例患者行LVAD植入术,中位年龄54岁,男性占51.52%。缺血性心肌病是主要病因(27.27%)。中位体外循环(CPB)时间153 min (IQR: 128 ~ 181)。体外循环期间乳酸水平中位数为1.8 mmol/L (IQR: 1.5-2.2),心脏指数最小CI为2.3至最大CI为2.6 L/min/m2。结论本研究强调了心肺灌注在晚期心力衰竭患者长期lvad植入成功中的重要作用。最佳术中管理,包括控制温度、低乳酸水平和最佳心脏指数,强调需要标准化的策略和灌注师的专业知识。
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引用次数: 0
VV-ECMO cannulation-related right brachiocephalic vein injury associated with pleural empyema. VV-ECMO插管相关右头臂静脉损伤伴胸膜脓肿。
IF 1.1 4区 医学 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-04 DOI: 10.1177/02676591251415345
Akira Kono, Philip Hawke, Koichi Haruta, Akihiro Miyake

IntroductionThe benefits of veno-venous extracorporeal membrane oxygenation (VV-ECMO) for patients with acute respiratory distress syndrome (ARDS) are well established. However, cannulation-related vascular complications, while rare, can be life-threatening.Case ReportAn 82-year-old man with ARDS caused by pleural empyema and lung abscess required VV-ECMO for worsening acidemia and hypoxemia. During internal jugular vein cannulation, a purulent effusion abruptly emerged from the outflow catheter. CT revealed catheter perforation of the brachiocephalic vein with fistulization into the pleural empyema. ECMO support was re-established using an alternative configuration. Following surgical repair, the patient gradually recovered to ambulatory discharge.DiscussionCatheter penetration into a pleural empyema in the absence of congenital anomalies is extremely rare. Here, inflammation-related vascular fragility likely contributed. This highlights the importance of considering intrathoracic pathology when determining ECMO configuration.ConclusionPleural empyema may predispose patients to vascular complications associated with VV-ECMO. A tailored ECMO configuration is essential.

静脉-静脉体外膜氧合(VV-ECMO)治疗急性呼吸窘迫综合征(ARDS)患者的益处已得到充分证实。然而,插管相关的血管并发症虽然罕见,但可能危及生命。病例报告一例82岁男性胸膜脓肿和肺脓肿所致急性呼吸窘迫综合征(ARDS),因酸血症和低氧血症恶化需行VV-ECMO。颈内静脉插管时,流出导管突然出现化脓性积液。CT示导管头臂静脉穿孔,胸膜脓肿处形成瘘口。使用替代配置重新建立ECMO支持。手术修复后,患者逐渐恢复,可门诊出院。讨论在没有先天性异常的情况下,导管插入胸膜脓肿是非常罕见的。在这里,炎症相关的血管脆弱可能起了作用。这突出了在确定ECMO配置时考虑胸内病理的重要性。结论胸膜脓胸易引起VV-ECMO相关血管并发症。量身定制的ECMO配置至关重要。
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引用次数: 0
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